228115-75-1 Usage
Uses
Used in Pharmaceutical Industry:
.beta.-D-Galactopyranose, 1,6-dideoxy-2-O-(1,1-dimethylethyl)dimethylsilyl-1,6-epithio-3-O-(4-methoxyphenyl)methyl-, acetate is used as a building block for the synthesis of complex pharmaceutical molecules. Its unique structure and reactivity make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, .beta.-D-Galactopyranose, 1,6-dideoxy-2-O-(1,1-dimethylethyl)dimethylsilyl-1,6-epithio-3-O-(4-methoxyphenyl)methyl-, acetate is used as a starting material for the synthesis of bioactive compounds with potential applications in pest control, crop protection, and other agricultural areas.
Used in Materials Science:
.beta.-D-Galactopyranose, 1,6-dideoxy-2-O-(1,1-dimethylethyl)dimethylsilyl-1,6-epithio-3-O-(4-methoxyphenyl)methyl-, acetate is employed in materials science for the development of novel materials with specific properties. Its unique structure allows for the creation of materials with tailored characteristics, such as improved mechanical strength, thermal stability, or biocompatibility.
Organic Synthesis:
.beta.-D-Galactopyranose, 1,6-dideoxy-2-O-(1,1-dimethylethyl)dimethylsilyl-1,6-epithio-3-O-(4-methoxyphenyl)methyl-, acetate is used as a key intermediate in organic synthesis, particularly for the preparation of complex organic molecules with diverse applications across various industries. Its versatility and reactivity make it an essential component in the synthesis of target compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 228115-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,1,1 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 228115-75:
(8*2)+(7*2)+(6*8)+(5*1)+(4*1)+(3*5)+(2*7)+(1*5)=121
121 % 10 = 1
So 228115-75-1 is a valid CAS Registry Number.
228115-75-1Relevant academic research and scientific papers
Synthesis studies of structural analogues of tagetitoxin: 4-O-acetyl-3- amino-1,6-anhydro-3-deoxy-D-gulose 2-phosphate
Dent, Barry R.,Furneaux, Richard H.,Gainsford, Graeme J.,Lynch, Gregory P.
, p. 6977 - 6996 (2007/10/03)
Synthetic approaches to structural analogues of tagetitoxin (1) are described. The successful route to analogue 3 (X=O) has, as a key step, protection of the cis-vicinal amino alcohol moiety of compound 7 as an N- benzylated cyclic carbamate (9). X-Ray cr
